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. 2011 May 13;88(5):677. doi: 10.1016/j.ajhg.2011.04.020

Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly

Fowzan S Alkuraya, Xuyu Cai, Carina Emery, Ganeshwaran H Mochida, Mohammed S Al-Dosari, Jillian M Felie, R Sean Hill, Brenda J Barry, Jennifer N Partlow, Generoso G Gascon, Amal Kentab, Mohammad Jan, Ranad Shaheen, Yuanyi Feng ∗, Christopher A Walsh ∗∗
PMCID: PMC3146721

(The American Journal of Human Genetics, 88, 536–547; May 13, 2011)

In the original version of this article, the title was incorrectly written as “Human Mutations in the NDE1 Cause Extreme Microcephaly with Lissencephaly.” This error has been corrected in both the online and the print version. The journal regrets the error.

Contributor Information

Yuanyi Feng, Email: yuanyi-feng@northwestern.edu.

Christopher A. Walsh, Email: christopher.walsh@childrens.harvard.edu.

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

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